A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028412



Internal ID20595452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13569885..13588142hg38UCSC Ensembl
chr16:13663742..13681999hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3818258
hg1918258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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